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Subscribe To Our Syndicated NewsStore-Brand Acetaminophen Caplets Recalled
-November 9, 2006
The U.S. Food and Drug Administration issued an alert today, notifying the public of the immediate recall of approximately 11 million bottles of various store-brand 500mg acetaminophen caplets.
According to the FDA, Perrigo Company decided to conduct a voluntary recall of the caplets after discovering that some were contaminated with metal fragments ranging in size from microdots to segments of wire measuring eight millimeters in length.
Officials at both the FDA and Perrigo said the source of contamination was being investigated. However, in its original report to the FDA, Perrigo suggested that the contamination was the result of prematurely worn down tableting equipment.
What Consumers Should Know
The FDA said it has not received reports of any adverse health events related to this recall and added that the risk of illness or injury is small. However, consumers who experience stomach discomfort, cuts to the throat or mouth, or other serious reaction are urged to contact a physician.
Consumers are also encouraged to report any adverse reactions to the FDA's MedWatch Program. Those who believe they possess an affected batch should contact Perrigo's Consumer Affairs Department at 877-546-0454.
More than 380 lots are subject to recall. For a list of batches and store-brands affected, please visit the FDA website at www.fda.gov .
Injured by acetaminophen? Please contact us today to learn more about recovering your losses through a personal injury lawsuit.
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